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Wagner-Drouet, Eva Maria ; Teschner, Daniel ; Wolschke, Christine ; Janson, Dietlinde ; Schäfer-Eckart, Kerstin ; Gärtner, Johannes ; Mielke, Stephan ; Schreder, Martin ; Kobbe, Guido ; Kondakci, Mustafa ; Hilgendorf, Inken ; von Lilienfeld-Toal, Marie ; Klein, Stefan ; Heidenreich, Daniela ; Kreil, Sebastian ; Verbeek, Mareike ; Graß, Sandra ; Ditschkowski, Markus ; Gromke, Tanja ; Koch, Martina ; Lindemann, Monika ; Hünig, Thomas ; Schmidt, Traudel ; Rascle, Anne ; Guldan, Harald ; Barabas, Harald ; Deml, Ludwig ; Wagner, Ralf ; Wolff, Daniel

Standardized monitoring of cytomegalovirus-specific immunity can improve risk stratification of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation

Wagner-Drouet, Eva Maria, Teschner, Daniel , Wolschke, Christine, Janson, Dietlinde, Schäfer-Eckart, Kerstin, Gärtner, Johannes, Mielke, Stephan , Schreder, Martin, Kobbe, Guido, Kondakci, Mustafa, Hilgendorf, Inken , von Lilienfeld-Toal, Marie, Klein, Stefan, Heidenreich, Daniela, Kreil, Sebastian, Verbeek, Mareike, Graß, Sandra, Ditschkowski, Markus, Gromke, Tanja, Koch, Martina, Lindemann, Monika , Hünig, Thomas, Schmidt, Traudel, Rascle, Anne , Guldan, Harald, Barabas, Harald, Deml, Ludwig, Wagner, Ralf und Wolff, Daniel (2021) Standardized monitoring of cytomegalovirus-specific immunity can improve risk stratification of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation. Haematologica 106 (2), S. 363-374.

Veröffentlichungsdatum dieses Volltextes: 15 Mrz 2023 16:13
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.45155


Zusammenfassung

Recurrence of cytomegalovirus reactivation remains a major cause of morbidity and mortality following allogeneic hematopoietic stem cell transplantation. Monitoring cytomegalovirus-specific cellular immunity using a standardized assay might improve the risk stratification of patients. A prospective multicenter study was conducted in 175 intermediate- and high-risk allogeneic hematopoietic stem ...

Recurrence of cytomegalovirus reactivation remains a major cause of morbidity and mortality following allogeneic hematopoietic stem cell transplantation. Monitoring cytomegalovirus-specific cellular immunity using a standardized assay might improve the risk stratification of patients. A prospective multicenter study was conducted in 175 intermediate- and high-risk allogeneic hematopoietic stem cell transplant recipients under preemptive antiviral therapy. Cytomegalovirus-specific cellular immunity was measured using a standardized interferon. enzyme-linked immunospot assay (T-Track (R) CMV). The primary aim was to evaluate the suitability of measuring cytomegalovirus-specific immunity after the end of treatment for a first cytomegalovirus reactivation to predict recurrent reactivation. Forty of 101 (39.6%) patients with a first cytomegalovirus reactivation experienced recurrent reactivations, mainly in the high-risk group (cytomegalovirus-seronegative donor/cytomegalovirus-seropositive recipient). The positive predictive value of T-Track (R) CMV (patients with a negative test after the first reactivation who experienced at least one recurrent reactivation) was 84.2% in high-risk patients. Kaplan-Meier analysis revealed a higher probability of recurrent cytomegalovirus reactivation in high-risk patients with a negative test after the first reactivation (hazard ratio 2.73; P=0.007). Interestingly, a post-hoc analysis considering T-Track (R) CMV measurements at day 100 after transplantation, a time point highly relevant for outpatient care, showed a positive predictive value of 90.0% in high-risk patients. Our results indicate that standardized cytomegalovirus-specific cellular immunity monitoring may allow improved risk stratification and management of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftHaematologica
Verlag:Ferrata-Storti Foundation
Ort der Veröffentlichung:PAVIA
Band:106
Nummer des Zeitschriftenheftes oder des Kapitels:2
Seitenbereich:S. 363-374
DatumFebruar 2021
InstitutionenMedizin > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Medizin > Lehrstuhl für Medizinische Mikrobiologie und Hygiene
Identifikationsnummer
WertTyp
10.3324/haematol.2019.229252DOI
Stichwörter / KeywordsCD8(+) T-CELLS; IDENTIFY PATIENTS; QUANTIFERON-CMV; RECONSTITUTION; RECIPIENTS; INFECTION; DISEASE; CD4(+); RESPONSES; ASSAY;
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-451554
Dokumenten-ID45155

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